CA2571306A1 - Agents epaississants a base de polyurethane - Google Patents

Agents epaississants a base de polyurethane Download PDF

Info

Publication number: CA2571306A1
Authority: CA; Canada
Prior art keywords: groups; compounds; water; thickeners; per molecule
Prior art date: 2004-07-01
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Granted

Application number

CA002571306A

Other languages

English (en)

Other versions

CA2571306C (fr

Inventor

Ludwig Schieferstein

Oliver Pietsch

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Cognis IP Management GmbH

Original Assignee

Individual

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2004-07-01

Filing date

2005-06-22

Publication date

2006-01-12

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34982466&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CA2571306(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2005-06-22 Application filed by Individual filed Critical Individual

2006-01-12 Publication of CA2571306A1 publication Critical patent/CA2571306A1/fr

2013-02-12 Application granted granted Critical

2013-02-12 Publication of CA2571306C publication Critical patent/CA2571306C/fr

2025-06-22 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000002562 thickening agent Substances 0.000 title claims abstract description 36
239000004814 polyurethane Substances 0.000 title claims abstract description 30
229920002635 polyurethane Polymers 0.000 title claims abstract description 30
150000001875 compounds Chemical class 0.000 claims abstract description 56
230000002209 hydrophobic effect Effects 0.000 claims abstract description 36
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 31
239000012948 isocyanate Substances 0.000 claims abstract description 22
150000002513 isocyanates Chemical class 0.000 claims abstract description 21
125000000524 functional group Chemical group 0.000 claims abstract description 12
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 11
239000006185 dispersion Substances 0.000 claims abstract description 11
229920005862 polyol Polymers 0.000 claims abstract description 11
150000003077 polyols Chemical class 0.000 claims abstract description 11
229920006395 saturated elastomer Polymers 0.000 claims abstract description 9
230000008719 thickening Effects 0.000 claims abstract description 9
125000005842 heteroatom Chemical group 0.000 claims abstract description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
238000002360 preparation method Methods 0.000 claims abstract description 7
125000001033 ether group Chemical group 0.000 claims abstract description 6
125000000217 alkyl group Chemical group 0.000 claims abstract description 5
150000002433 hydrophilic molecules Chemical class 0.000 claims abstract description 5
150000001298 alcohols Chemical class 0.000 claims description 34
238000006243 chemical reaction Methods 0.000 claims description 31
229920001223 polyethylene glycol Polymers 0.000 claims description 28
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 14
239000005058 Isophorone diisocyanate Substances 0.000 claims description 11
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
239000005977 Ethylene Substances 0.000 claims description 6
239000003973 paint Substances 0.000 claims description 5
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 4
239000012141 concentrate Substances 0.000 claims description 4
239000002537 cosmetic Substances 0.000 claims description 4
239000000839 emulsion Substances 0.000 claims description 4
125000004185 ester group Chemical group 0.000 claims description 4
239000003960 organic solvent Substances 0.000 claims description 4
239000002736 nonionic surfactant Substances 0.000 claims description 3
239000008096 xylene Substances 0.000 claims description 3
238000004140 cleaning Methods 0.000 claims description 2
239000008199 coating composition Substances 0.000 claims description 2
150000002191 fatty alcohols Chemical class 0.000 claims description 2
229920000642 polymer Polymers 0.000 description 19
239000000047 product Substances 0.000 description 18
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
239000002202 Polyethylene glycol Substances 0.000 description 14
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 12
125000005442 diisocyanate group Chemical group 0.000 description 12
239000000203 mixture Substances 0.000 description 12
GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 10
NNOZGCICXAYKLW-UHFFFAOYSA-N 1,2-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC=C1C(C)(C)N=C=O NNOZGCICXAYKLW-UHFFFAOYSA-N 0.000 description 9
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
239000008367 deionised water Substances 0.000 description 9
229910021641 deionized water Inorganic materials 0.000 description 9
229910052739 hydrogen Inorganic materials 0.000 description 9
239000001257 hydrogen Substances 0.000 description 9
238000004519 manufacturing process Methods 0.000 description 9
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
239000000126 substance Substances 0.000 description 8
-1 amino, imino Chemical group 0.000 description 7
229910052757 nitrogen Inorganic materials 0.000 description 7
229920000151 polyglycol Polymers 0.000 description 7
239000010695 polyglycol Substances 0.000 description 7
AZYRZNIYJDKRHO-UHFFFAOYSA-N 1,3-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC(C(C)(C)N=C=O)=C1 AZYRZNIYJDKRHO-UHFFFAOYSA-N 0.000 description 6
XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 6
PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 6
239000003054 catalyst Substances 0.000 description 6
239000003085 diluting agent Substances 0.000 description 6
238000000034 method Methods 0.000 description 6
239000002904 solvent Substances 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
239000004440 Isodecyl alcohol Substances 0.000 description 5
238000009472 formulation Methods 0.000 description 5
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 5
229920000570 polyether Polymers 0.000 description 5
239000005056 polyisocyanate Substances 0.000 description 5
229920001228 polyisocyanate Polymers 0.000 description 5
239000005057 Hexamethylene diisocyanate Substances 0.000 description 4
239000004721 Polyphenylene oxide Substances 0.000 description 4
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 4
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
238000003756 stirring Methods 0.000 description 4
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 4
FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000004411 aluminium Substances 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
239000000470 constituent Substances 0.000 description 3
KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
230000035484 reaction time Effects 0.000 description 3
VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 2
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
XKGDWZQXVZSXAO-ADYSOMBNSA-N Ricinoleic Acid methyl ester Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OC XKGDWZQXVZSXAO-ADYSOMBNSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
238000007605 air drying Methods 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
150000002009 diols Chemical class 0.000 description 2
238000001035 drying Methods 0.000 description 2
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
239000011261 inert gas Substances 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
238000006384 oligomerization reaction Methods 0.000 description 2
239000000049 pigment Substances 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000000376 reactant Substances 0.000 description 2
230000003134 recirculating effect Effects 0.000 description 2
XKGDWZQXVZSXAO-UHFFFAOYSA-N ricinoleic acid methyl ester Natural products CCCCCCC(O)CC=CCCCCCCCC(=O)OC XKGDWZQXVZSXAO-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 2
SSUJUUNLZQVZMO-UHFFFAOYSA-N 1,2,3,4,8,9,10,10a-octahydropyrimido[1,2-a]azepine Chemical compound C1CCC=CN2CCCNC21 SSUJUUNLZQVZMO-UHFFFAOYSA-N 0.000 description 1
XIUYWALZDCQJCF-UHFFFAOYSA-N 1,2-diisocyanatododecane Chemical compound CCCCCCCCCCC(N=C=O)CN=C=O XIUYWALZDCQJCF-UHFFFAOYSA-N 0.000 description 1
ZTNJGMFHJYGMDR-UHFFFAOYSA-N 1,2-diisocyanatoethane Chemical compound O=C=NCCN=C=O ZTNJGMFHJYGMDR-UHFFFAOYSA-N 0.000 description 1
VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
ATOUXIOKEJWULN-UHFFFAOYSA-N 1,6-diisocyanato-2,2,4-trimethylhexane Chemical compound O=C=NCCC(C)CC(C)(C)CN=C=O ATOUXIOKEJWULN-UHFFFAOYSA-N 0.000 description 1
QGLRLXLDMZCFBP-UHFFFAOYSA-N 1,6-diisocyanato-2,4,4-trimethylhexane Chemical compound O=C=NCC(C)CC(C)(C)CCN=C=O QGLRLXLDMZCFBP-UHFFFAOYSA-N 0.000 description 1
AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 1
LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
VZDIRINETBAVAV-UHFFFAOYSA-N 2,4-diisocyanato-1-methylcyclohexane Chemical compound CC1CCC(N=C=O)CC1N=C=O VZDIRINETBAVAV-UHFFFAOYSA-N 0.000 description 1
UZVAZDQMPUOHKP-UHFFFAOYSA-N 2-(7-methyloctyl)phenol Chemical compound CC(C)CCCCCCC1=CC=CC=C1O UZVAZDQMPUOHKP-UHFFFAOYSA-N 0.000 description 1
IMVGFDIQASHWEF-UHFFFAOYSA-N 2-ethylhexanoic acid;methane Chemical compound C.C.CCCCC(CC)C(O)=O IMVGFDIQASHWEF-UHFFFAOYSA-N 0.000 description 1
BOZRCGLDOHDZBP-UHFFFAOYSA-N 2-ethylhexanoic acid;tin Chemical compound [Sn].CCCCC(CC)C(O)=O BOZRCGLDOHDZBP-UHFFFAOYSA-N 0.000 description 1
125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
229920005682 EO-PO block copolymer Polymers 0.000 description 1
238000003547 Friedel-Crafts alkylation reaction Methods 0.000 description 1
238000007869 Guerbet synthesis reaction Methods 0.000 description 1
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
IIGAAOXXRKTFAM-UHFFFAOYSA-N N=C=O.N=C=O.CC1=C(C)C(C)=C(C)C(C)=C1C Chemical compound N=C=O.N=C=O.CC1=C(C)C(C)=C(C)C(C)=C1C IIGAAOXXRKTFAM-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004435 Oxo alcohol Substances 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
238000006853 Ziegler synthesis reaction Methods 0.000 description 1
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 description 1
GPDWNEFHGANACG-UHFFFAOYSA-L [dibutyl(2-ethylhexanoyloxy)stannyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)O[Sn](CCCC)(CCCC)OC(=O)C(CC)CCCC GPDWNEFHGANACG-UHFFFAOYSA-L 0.000 description 1
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
239000013543 active substance Substances 0.000 description 1
238000007259 addition reaction Methods 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
QAEKNCDIHIGLFI-UHFFFAOYSA-L cobalt(2+);2-ethylhexanoate Chemical compound [Co+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O QAEKNCDIHIGLFI-UHFFFAOYSA-L 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
150000001983 dialkylethers Chemical class 0.000 description 1
239000012975 dibutyltin dilaurate Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000539 dimer Substances 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
PBJZAYSKNIIHMZ-UHFFFAOYSA-N ethyl carbamate;oxirane Chemical class C1CO1.CCOC(N)=O PBJZAYSKNIIHMZ-UHFFFAOYSA-N 0.000 description 1
229920001038 ethylene copolymer Polymers 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
235000019387 fatty acid methyl ester Nutrition 0.000 description 1
239000000945 filler Substances 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
238000010559 graft polymerization reaction Methods 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
WMIYKQLTONQJES-UHFFFAOYSA-N hexafluoroethane Chemical compound FC(F)(F)C(F)(F)F WMIYKQLTONQJES-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
238000007037 hydroformylation reaction Methods 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
238000006317 isomerization reaction Methods 0.000 description 1
VXWPONVCMVLXBW-UHFFFAOYSA-M magnesium;carbanide;iodide Chemical compound [CH3-].[Mg+2].[I-] VXWPONVCMVLXBW-UHFFFAOYSA-M 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000008194 pharmaceutical composition Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920001610 polycaprolactone Polymers 0.000 description 1
239000004632 polycaprolactone Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229940096992 potassium oleate Drugs 0.000 description 1
MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
238000005070 sampling Methods 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
239000004753 textile Substances 0.000 description 1
YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
229950006389 thiodiglycol Drugs 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
229940087291 tridecyl alcohol Drugs 0.000 description 1
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
239000013638 trimer Substances 0.000 description 1
238000010518 undesired secondary reaction Methods 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
239000001993 wax Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/87—Polyurethanes
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/2815—Monohydroxy compounds
- C08G18/282—Alkanols, cycloalkanols or arylalkanols including terpenealcohols
- C08G18/2825—Alkanols, cycloalkanols or arylalkanols including terpenealcohols having at least 6 carbon atoms
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/751—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
- C08G18/752—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
- C08G18/753—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
- C08G18/755—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7614—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring
- C08G18/7628—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring containing at least one isocyanate or isothiocyanate group linked to the aromatic ring by means of an aliphatic group
- C08G18/765—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring containing at least one isocyanate or isothiocyanate group linked to the aromatic ring by means of an aliphatic group alpha, alpha, alpha', alpha', -tetraalkylxylylene diisocyanate or homologues substituted on the aromatic ring
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/43—Thickening agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/48—Thickener, Thickening system
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Dermatology (AREA)
Birds (AREA)
Epidemiology (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Polyurethanes Or Polyureas (AREA)
Cosmetics (AREA)
Paints Or Removers (AREA)

CA2571306A 2004-07-01 2005-06-22 Agents epaississants a base de polyurethane Expired - Fee Related CA2571306C (fr)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE102004031786.0		2004-07-01
DE102004031786A DE102004031786A1 (de)	2004-07-01	2004-07-01	Verdickungsmittel auf Polyurethanbasis
PCT/EP2005/006743 WO2006002813A2 (fr)	2004-07-01	2005-06-22	Agents epaississants a base de polyurethane

Publications (2)

Publication Number	Publication Date
CA2571306A1 true CA2571306A1 (fr)	2006-01-12
CA2571306C CA2571306C (fr)	2013-02-12

Family

ID=34982466

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA2571306A Expired - Fee Related CA2571306C (fr)	2004-07-01	2005-06-22	Agents epaississants a base de polyurethane

Country Status (8)

Country	Link
US (1)	US8334357B2 (fr)
EP (1)	EP1765900B1 (fr)
JP (1)	JP4977018B2 (fr)
CN (1)	CN1980968B (fr)
CA (1)	CA2571306C (fr)
DE (2)	DE102004031786A1 (fr)
ES (1)	ES2354078T3 (fr)
WO (1)	WO2006002813A2 (fr)

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB0222522D0 (en)	2002-09-27	2002-11-06	Controlled Therapeutics Sct	Water-swellable polymers
GB0417401D0 (en)	2004-08-05	2004-09-08	Controlled Therapeutics Sct	Stabilised prostaglandin composition
GB0613333D0 (en)	2006-07-05	2006-08-16	Controlled Therapeutics Sct	Hydrophilic polyurethane compositions
GB0613638D0 (en)	2006-07-08	2006-08-16	Controlled Therapeutics Sct	Polyurethane elastomers
GB0620685D0 (en)	2006-10-18	2006-11-29	Controlled Therapeutics Sct	Bioresorbable polymers
DE102006056509A1 (de) *	2006-11-30	2008-06-05	Evonik Goldschmidt Gmbh	Polyurethan-Verdickungsmittel zur Verdickung wässriger Systeme
CN101600415A (zh) *	2007-01-31	2009-12-09	巴斯夫欧洲公司	阳离子调理剂
EP2282715B1 (fr) *	2008-05-06	2018-03-07	Basf Se	Polyuréthanes comme agents modificateurs de rhéologie pour préparations cosmétiques
EP2184304A1 (fr)	2008-05-06	2010-05-12	Basf Se	Epaississeur de polyuréthane
US7868122B2 (en) *	2008-06-19	2011-01-11	Southern Clay Products, Inc.	Tint-viscosity stabilization polymeric thickeners
EP2305728B1 (fr) *	2009-10-02	2015-09-02	Cognis IP Management GmbH	Epaississant
EP2327732A1 (fr) *	2009-11-27	2011-06-01	Cognis IP Management GmbH	Épaississant à base de polyuréthane
CN102101909B (zh) *	2009-12-18	2012-11-21	广州熵能聚合物技术有限公司	一种水溶性缔合型聚氨酯增稠剂及其反相聚合方法与应用
EP2361939B1 (fr)	2010-02-25	2012-08-22	Cognis IP Management GmbH	Epaississant à base de polyuréthane
US20120082629A1 (en) *	2010-09-01	2012-04-05	Basf Se	Associative Thickeners For Aqueous Preparations
MX2013002262A (es)	2010-09-01	2013-05-22	Basf Se	Espesante asociativo para preparaciones acuosas.
KR101834593B1 (ko)	2010-10-22	2018-03-05	바스프 에스이	폴리우레탄 증점제
US9175125B2 (en)	2010-10-22	2015-11-03	Basf Se	Polyurethane thickeners
JP6041807B2 (ja)	2010-10-22	2016-12-14	ビーエイエスエフ・ソシエタス・エウロパエアＢａｓｆＳｅ	ポリウレタン増粘剤
US8871817B2 (en)	2010-10-22	2014-10-28	Basf Se	Polyurethane thickeners
WO2012096124A1 (fr) *	2011-01-13	2012-07-19	住友精化株式会社	Produit de modification d'oxyde polyalkylène hydrosoluble
JP2014504668A (ja)	2011-01-20	2014-02-24	ビーエイエスエフ・ソシエタス・エウロパエア	樹枝状ポリエーテル−ポリウレタン増粘剤
US9066891B2 (en)	2011-01-20	2015-06-30	Base Se	Dendritic polyether-polyurethane thickeners
JP5855437B2 (ja) *	2011-12-01	2016-02-09	住友精化株式会社	水溶性ポリアルキレンオキシド変性物
CN104169352B (zh) *	2012-03-08	2016-08-31	赫尔克里士公司	使用有机磷酸酯对缔合型增稠剂进行粘度抑制
IN2014DE02424A (fr) *	2013-10-28	2015-07-10	Rohm & Haas
BR112016025760A8 (pt)	2014-05-05	2021-05-04	Resinate Mat Group Inc	processo, polióis de poliéster, poliuretano e resina curável
EP3226836A1 (fr) *	2014-12-04	2017-10-11	Lubrizol Advanced Materials, Inc.	Modification de la viscosité de compositions contenant une phase organique
WO2016153780A1 (fr)	2015-03-20	2016-09-29	Resinate Materials Group, Inc.	Polyols de polyester cycloaliphatique à partir de polyesters thermoplastiques
US9522976B2 (en)	2015-03-20	2016-12-20	Resinate Materials Group, Inc.	Cycloaliphatic polyester polyols from thermoplastic polyesters
FR3041964B1 (fr) *	2015-10-05	2017-10-20	Coatex Sas	Agent epaississant pour systemes aqueux, formulations le contenant et utilisations.
EP3508194B1 (fr)	2016-08-31	2021-06-16	Adeka Corporation	Composition aqueuse d'agent gélifiant et préparation cosmétique l'utilisant
CN109996847B (zh)	2016-10-07	2021-07-09	巴斯夫欧洲公司	含二氧化钛颜料的乳胶漆
EP3672922A4 (fr)	2017-08-22	2021-05-05	3M Innovative Properties Company	Composés muraux et leurs procédés d'utilisation
EP3707183B1 (fr) *	2017-11-08	2022-01-05	Basf Se	Additifs polymères permettant de réduire la perte de viscosité sur une teinture
ES2966064T3 (es)	2018-08-02	2024-04-18	Basf Se	Procedimiento para producir una dispersión polimérica acuosa
ES2946660T3 (es)	2019-05-08	2023-07-24	Basf Se	Látex polimérico acuoso
ES2966171T3 (es)	2019-07-26	2024-04-18	Basf Se	Proceso de producción de una dispersión polimérica acuosa
US20220289896A1 (en) *	2019-08-08	2022-09-15	Byk-Chemie Gmbh	Additive for temperature adaptive rheology profile
CN110746812B (zh) *	2019-11-04	2022-02-15	万华化学集团股份有限公司	含非离子聚氨酯化合物的触变混合物及包括其的水性皮革表面处理涂料
CN115087710B (zh) *	2020-03-31	2024-03-01	科莱恩国际有限公司	疏水改性聚氨酯增稠剂及其制备方法
US11845863B2 (en)	2020-05-04	2023-12-19	Carlisle Construction Materials, LLC	Polyurethane dispersions and their use to produce coatings and adhesives
WO2021228804A1 (fr)	2020-05-12	2021-11-18	U. Windmöller Innovation Gmbh & Co. Kg	Procédé de production de polyols à base d'acide gras hydroxylé
MX2023000894A (es)	2020-07-20	2023-02-22	Basf Se	Latex de polimero acuoso de copolimeros formadores de pelicula adecuado como aglutinante en composiciones de recubrimiento a base de agua.
CN116806228A (zh)	2021-01-26	2023-09-26	巴斯夫欧洲公司	水性聚合物胶乳
FI4381012T3 (fi)	2021-08-04	2025-12-08	Basf Se	Menetelmä vesipitoisen polymeerilateksin modifioimiseksi
US20250171645A1 (en) *	2022-03-08	2025-05-29	Unilin, Bv	Use of a hydrophobic polymer on decorative panels and method
BE1030344B1 (nl) *	2022-03-15	2023-10-16	Flooring Ind Ltd Sarl	Gebruik van een hydrofoob polymeer bij decoratieve panelen en werkwijze
WO2024105095A1 (fr)	2022-11-18	2024-05-23	Basf Se	Latex polymère aqueux de copolymères filmogènes approprié comme liant dans des compositions de revêtement à base aqueuse
CN116355169B (zh) *	2023-03-09	2025-01-03	亚培烯科技(上海)有限公司	聚合物及其制备方法和用途
TW202502831A (zh)	2023-03-24	2025-01-16	德商巴斯夫歐洲公司	適合作為水性塗料組成物中黏合劑的成膜共聚物的水性聚合物膠乳
CN116769130A (zh) *	2023-06-12	2023-09-19	上海奕朗化工有限公司	混合封端聚氨酯缔合型增稠剂及制备方法
TW202509091A (zh)	2023-08-16	2025-03-01	德商巴斯夫歐洲公司	適合作為水性塗料組成物中之黏合劑之共聚物之含水聚合物乳膠
WO2025125496A1 (fr)	2023-12-13	2025-06-19	Basf Se	Latex polymère aqueux de copolymères approprié en tant que liant dans des compositions de revêtement à base d'eau
WO2025132646A1 (fr)	2023-12-19	2025-06-26	Basf Se	Compositions de revêtement à l'eau nécessitant des quantités réduites de biocides

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4079028A (en)	1975-10-03	1978-03-14	Rohm And Haas Company	Polyurethane thickeners in latex compositions
JPS6049022A (ja) *	1983-08-29	1985-03-18	Sannopuko Kk	優れた調色性およびレベリング性を与える増粘性組成物
DE4137247A1 (de)	1991-11-13	1993-05-19	Henkel Kgaa	Verdickungsmittel auf polyurethanbasis
DE4327481A1 (de) *	1993-08-16	1995-02-23	Bayer Ag	Als Verdickungsmittel geeignete Polyurethane und ihre Verwendung zur Verdickung wäßriger Systeme
DE19604466A1 (de)	1996-02-08	1997-08-14	Basf Ag	Wässerige Zubereitungen, enthaltend Alkylpolyglykoside und ein Polymer
KR100613969B1 (ko) *	1998-12-17	2006-08-18	가부시키가이샤 시세이도	화장료 조성물
JP4289571B2 (ja) *	1999-02-25	2009-07-01	株式会社Ａｄｅｋａ	粘性調整剤
FR2811993B1 (fr) *	2000-07-21	2006-08-04	Oreal	Nouveaux polymeres associatifs cationiques et leur utilisation comme epaississants
JP2002226542A (ja) *	2001-01-30	2002-08-14	Asahi Denka Kogyo Kk	増粘、粘性調整剤
DE102004008015A1 (de) *	2004-02-19	2005-09-08	Cognis Deutschland Gmbh & Co. Kg	Verdickungsmittel für Polyurethanbasis

2004
- 2004-07-01 DE DE102004031786A patent/DE102004031786A1/de not_active Withdrawn
2005
- 2005-06-22 CN CN2005800224209A patent/CN1980968B/zh not_active Expired - Fee Related
- 2005-06-22 EP EP05746591A patent/EP1765900B1/fr not_active Revoked
- 2005-06-22 US US11/630,069 patent/US8334357B2/en not_active Expired - Fee Related
- 2005-06-22 ES ES05746591T patent/ES2354078T3/es not_active Expired - Lifetime
- 2005-06-22 DE DE502005010345T patent/DE502005010345D1/de not_active Expired - Lifetime
- 2005-06-22 JP JP2007519661A patent/JP4977018B2/ja not_active Expired - Lifetime
- 2005-06-22 CA CA2571306A patent/CA2571306C/fr not_active Expired - Fee Related
- 2005-06-22 WO PCT/EP2005/006743 patent/WO2006002813A2/fr not_active Ceased

Also Published As

Publication number	Publication date
ES2354078T3 (es)	2011-03-09
CN1980968B (zh)	2010-05-05
JP4977018B2 (ja)	2012-07-18
US20080108775A1 (en)	2008-05-08
JP2008505232A (ja)	2008-02-21
DE102004031786A1 (de)	2006-01-26
WO2006002813A3 (fr)	2006-06-08
EP1765900A2 (fr)	2007-03-28
CA2571306C (fr)	2013-02-12
DE502005010345D1 (de)	2010-11-18
EP1765900B1 (fr)	2010-10-06
CN1980968A (zh)	2007-06-13
US8334357B2 (en)	2012-12-18
WO2006002813A2 (fr)	2006-01-12

Publication	Publication Date	Title
CA2571306C (fr)	2013-02-12	Agents epaississants a base de polyurethane
US20050187342A1 (en)	2005-08-25	Polyurethane-based thickeners
US8461213B2 (en)	2013-06-11	Thickeners based on polyurethane
KR100297345B1 (ko)	2001-10-24	폴리우레탄증점제및수성계의증점을위한그의용도
CN103159911B (zh)	2016-03-02	流变改性剂
US5500475A (en)	1996-03-19	Polyurethane-based thickeners
US20110130471A1 (en)	2011-06-02	Polyurethanes
CA2168405C (fr)	2007-08-28	Epaississants a base de polyurethane pour compositions aqueuses
KR101972185B1 (ko)	2019-04-24	시클로헥실올 알킬을 함유하는 비이온성 회합성 증점제, 이를 함유하는 제제 및 이들의 용도
JP4128785B2 (ja)	2008-07-30	新規ポリウレタンおよび水性系の増粘におけるその使用
US20070293625A1 (en)	2007-12-20	New polyurethanes and their use for thickening aqueous systems
KR101960118B1 (ko)	2019-03-19	시클로헥실올 알킬을 함유하는 비이온성 회합성 증점제, 이를 함유하는 제제 및 이들의 용도
JP4122165B2 (ja)	2008-07-23	新規ポリウレタンおよび水性系の増粘におけるその使用
DE102006023001A1 (de)	2007-11-22	Verdickungsmittel auf Polyurethanbasis
CN106916274B (zh)	2021-04-20	用于抗粘连性及凝固时间的聚醚-氨基甲酸酯-脲添加剂
KR101939868B1 (ko)	2019-01-17	알킬 사이클로헥산올 알콕실레이트를 포함하는 회합성 비이온성 증점제, 이들의 용도 및 이들을 포함하는 제제
KR19980018753A (ko)	1998-06-05	폴리우레탄 기재의 증점제 조성물 및 수성 조성물을 증점시키기 위한 그의 용도 (Polyurethane-based Thickener Compositions and Their Use for Thickening Aqueous Compositions)

Legal Events

Date	Code	Title	Description
2010-06-04	EEER	Examination request
2022-04-12	MKLA	Lapsed	Effective date: 20220301
2022-10-06	MKLA	Lapsed	Effective date: 20200831